NM_000288.4(PEX7):c.*305_*310del AND Phytanic acid storage disease

NM_000288.4(PEX7):c.305_310del AND Phytanic acid storage disease

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 14, 2016
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000274648.5

Allele description [Variation Report for NM_000288.4(PEX7):c.305_310del]

NM_000288.4(PEX7):c.305_310del

Gene:

PEX7:peroxisomal biogenesis factor 7 [Gene - OMIM - HGNC]

Variant type:

Deletion

Cytogenetic location:

6q23.3

Genomic location:

Preferred name:

NM_000288.4(PEX7):c.*305_*310del

HGVS:

NC_000006.12:g.136913831_136913836del
NG_008462.1:g.96252_96257del
NM_000288.4:c.*305_*310delMANE SELECT
NC_000006.11:g.137234969_137234974del
NM_000288.3:c.*305_*310delCTTATA

Links:

dbSNP: rs886061123

NCBI 1000 Genomes Browser:

rs886061123

Molecular consequence:

NM_000288.4:c.*305_*310del - 3 prime UTR variant - [Sequence Ontology: SO:0001624]

Condition(s)

Name:: Phytanic acid storage disease
Synonyms:: HMSN IV; REFSUM DISEASE, CLASSIC; Disorder of cornification 11 (phytanic acid type); See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0009958; MedGen: C0034960; Orphanet: 773; OMIM: 266500

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PREDICTED: Homo sapiens HPS4 biogenesis of lysosomal organelles complex 3 subuni...
PREDICTED: Homo sapiens HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 (HPS4), transcript variant X40, mRNA
gi|2462585804|ref|XM_054326082.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000460561	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification 20161018)	Uncertain significance (Jun 14, 2016)	germline	clinical testing	ICSL_Variant_Classification_20161018.pdf Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000460561

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification 20161018)

Uncertain significance
(Jun 14, 2016)

germline

clinical testing

ICSL_Variant_Classification_20161018.pdf

Citation Link

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Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Illumina Laboratory Services, Illumina, SCV000460561.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Apr 9, 2023

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